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Chick-Fil-A
Updated: September 22, 2020 12:00 PM
Covid-19 OSHA Complaint, Chick-fil-A, 7201 West Cermak Road, North Riverside, Riverside, Illinois 60546, USA
Chick-fil-A, 7201 West Cermak Road, North Riverside, Riverside, Illinois 60546, USA
September 22, 2020 12:00 PM
“1. The employer is not following CDC guidelines in regarding informing employees of workers who have tested positive for Covid-19. One employee(s) tested positive and the coworkers were not informed .
Applicable OSHA standard(s): Section 5(a)(1) General Duty Clause of the Occupational Safety and... See MoreHealth Act of 1970
2. The employer is not following CDC guidelines regarding to the use of facemasks or face coverings, the employer is not providing enough PPE to the employees and the managers are not properly wearing the facemasks when working in the restaurant.
Applicable OSHA standard(s): 1910.132
Alleged Hazards: 2, Employees Exposed: 80
Source: Osha.gov | Receipt Date: 2020-08-10 See Less”
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Covid-19 OSHA Complaint, Chick-fil-A, 805 Dawsonville Hwy, Gainesville, Georgia 30501, USA
Chick-fil-A, 805 Dawsonville Hwy, Gainesville, Georgia 30501, USA
September 22, 2020 12:00 PM
“The employer does not maintain an effective Infectious Disease Preparedness and Prevention Program for Covid-19. The employer does not inform workers of positive cases at the workplace. Sick employees are not isolated, and exposed employees are not identified, checked and quarantined. Masks are no... See Moret worn uniformly by all workers, and are not used as recommended for protection. Safe distancing is not practiced.
Alleged Hazards: 1, Employees Exposed: 30
Source: Osha.gov | Receipt Date: 2020-09-02 See Less”
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Employee tested positive for Covid-19, Chick-fil-A, Kingsville, TX 78363, United States
Chick-fil-A, Kingsville, TX 78363, United States
September 17, 2020 12:00 PM
“An employee at the Chick-fil-A in the Oklahoma Memorial Union food court has tested positive for COVID-19.
Source: oudaily.com See Less”
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Covid-19 OSHA Complaint, Chick-fil-A, 12160 Sunset Hills Rd, Reston, Virginia 20190, USA
Chick-fil-A, 12160 Sunset Hills Rd, Reston, Virginia 20190, USA
September 7, 2020 12:00 PM
“Employer is not screening employees prior to their shifts and ensuring that they stay home if experiencing signs and symptoms of COVID-19.
Employer is utilizing an inaccurate thermometer not set to measure the temperature of the human body.
Alleged Hazards: 2, Employees Exposed: 5
Source: Osh... See Morea.gov | Receipt Date: 2020-08-11 See Less”
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2 employees tested positive for Covid-19, Chick-fil-A, 9331 E Arapahoe Rd, Greenwood Village, CO 80112, USA
Chick-fil-A, 9331 E Arapahoe Rd, Greenwood Village, CO 80112, USA
September 2, 2020 12:00 PM
“2 employees at Chick-Fil-A 01304 Sept 2020 in Arapahoe county tested positive for Covid-19. The outbreak began on 8/28/2020
Source: colorado.gov See Less”
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Covid-19 OSHA Complaint, Chick-fil-A, 26792 Portola Parkway, Foothill Ranch, California 92610, USA
Chick-fil-A, 26792 Portola Parkway, Foothill Ranch, California 92610, USA
August 20, 2020 12:00 PM
“T8 CCR ? 3203(a)(2) ? Mask order not enforced in the restaurant by Employer.
Alleged Hazards: 1, Employees Exposed: 5
Source: Osha.gov | Receipt Date: 2020-07-07 See Less”
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Covid-19 OSHA Complaint, Chick-fil-A, 18521 Devonshire Street, Northridge, California 91324, USA
Chick-fil-A, 18521 Devonshire Street, Northridge, California 91324, USA
August 20, 2020 12:00 PM
“There is 4 known cases of COVID-19, but employees are not notified by management. The company as not been enforcing measures. The employees are not washing hands, people take off masks, and people take breaks not 6 ft. apart from each other. The employees have asked why the business has not shutdown... See More, on who has been exposed, not making employees be tested for virus.
Alleged Hazards: 1,
Source: Osha.gov | Receipt Date: 2020-06-16 See Less”
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Covid-19 OSHA Complaint, Chick-fil-A, 595 Northtown Drive Northeast, Blaine, Minnesota 55434, USA
Chick-fil-A, 595 Northtown Drive Northeast, Blaine, Minnesota 55434, USA
August 20, 2020 12:00 PM
“All employees are not wearing face masks as required by the CDC COVID-19 guidelines and the Executive order 20-81.
Source: Osha.gov | Receipt Date: 2020-07-30 See Less”
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Covid-19 OSHA Complaint, Chick-fil-A, 4779 Great Northern Blvd, North Olmsted, Ohio 44070, USA
Chick-fil-A, 4779 Great Northern Blvd, North Olmsted, Ohio 44070, USA
August 19, 2020 12:00 PM
“1. The face masks in use appear to be too thin or inadequate to protect the workers onsite. Additionally several workers do not wear them properly, i.e. under their noses, chins, etc. and are not told to put them on correctly.
2. Proper social distancing is not practiced on site as needed. Wo... See Morerkers are required to be close to customer's cars, well within the 6 foot recommendation.
Alleged Hazards: 2, Employees Exposed: 30
Source: Osha.gov | Receipt Date: 2020-07-28 See Less”
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Covid-19 OSHA Complaint, Chick-fil-A, Lenexa, Kansas, USA
Chick-fil-A, Lenexa, Kansas, USA
August 3, 2020 12:00 PM
“LENEXA, KS (KCTV) -- A local Chick-fil-A has had to close its doors after 10 cases of COVID-19 were tied to one location. During a meeting on Thursday, the Johnson County Board of Commissioners mentioned at least 10 cases are tied to a Chick-fil-A location in Lenexa. The restaurant's corporate site... See Moresays the location at 15919 W. 87th Street Parkway is closed due to "COVID-19 Related Issues." No word on how long the restaurant will have to be closed before reopening the location again.
Dear Employer:
On June 10, 2020, the Occupational Safety and Health Administration (OSHA) received a notification alleged workplace hazards(s) at your worksite concerning employees testing positive for Coronavirus.
The employer has had a confirmed COVID-19 cases at their Kansas facility. Employees are not protected from health hazards associated with the Coronavirus Disease 2019 (COVID-19). Employees are exposed in that the employer has not implemented all feasible engineering and administrative controls as outlined in the Centers for Disease Control and Prevention (CDC) guidelines, www.cdc.gov/coronavirus/2019-ncov/community/organizations/businesses-employers.html , and OSHA?s publication #3990-03 2020, Guidance on Preparing Workplaces for COVID-19, www.osha.gov/Publications/OSHA3990.pdf.
Section 5(a)(1) of the OSH Act.
We request that you immediately investigate??.
Source: Osha.gov | Receipt Date: 2020-06-22 See Less”
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Recent Interesting Reports
September 2, 2020 11:41 PM
“The FSA announced the recall of Lamb and Carrot Dumplings by Freshasia Foods because they contain crustaceans, which are not mentioned on the label. This means the product is a possible health risk for anyone with an allergy to crustaceans.
FSA advises consumers not to eat the recalled product. I... See Morenstead, return it to the store from where it was bought for a full refund.
+ Freshasia Lamb and Carrot Dumplings. 400g. Batch code: 200402. Best before: 6 April 2021
Freshasia Foods is recalling the above product from customers and has been advised to contact the relevant allergy support organisations, which will tell their members about the recall. The company has also issued a point-of-sale notice to its customers. These notices explain to customers why the product is being recalled and tell them what to do if they have bought the product.
Check the full recall details on food.gov.uk
Source: FSA See Less”
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September 17, 2020 11:00 PM
“Company name: Acella Pharmaceuticals, LLC
Brand name: NP Thyroid 15 & NP Thyroid120
Product recalled: Thyroid Tablets
Reason of the recall: Sub Potency
FDA Recall date: September 17, 2020
Recall details: Acella Pharmaceuticals, LLC is voluntarily recalling one lot of 15-mg and one lot of 120-mg... See MoreNP Thyroid®, Thyroid Tablets, USP [levothyroxine (T4) and liothyronine (T3)] to the consumer level. The products are being recalled because testing has found these lots to be sub potent. The product may have as low as 87% of the labeled amount of levothyroxine (T4). More information can be found at www.npthyroid.com/product-updates.
Risk Statement: Patients being treated for hypothyroidism (underactive thyroid), who receive sub potent NP Thyroid®, may experience signs and symptoms of hypothyroidism (underactive thyroid) which may include, fatigue, increased sensitivity to cold, constipation, dry skin, puffy face, hair loss, slow heart rate, depression, swelling of the thyroid gland and/or unexplained weight gain or difficulty losing weight. There is reasonable risk of serious injury in newborn infants or pregnant women with hypothyroidism including early miscarriage, fetal hyperthyroidism, and/or impairments to fetal neural and skeletal development. In elderly patients and patients with underlying cardiac disease toxic cardiac manifestations of hyperthyroidism may occur, such as cardiac pain, palpitations or cardiac arrhythmia.
To date, Acella has received four reports of adverse events for these lot numbers possibly related to this recall. NP Thyroid®, Thyroid Tablets, USP is composed of levothyroxine and liothyronine, and used to treat hypothyroidism (underactive thyroid). The products subject to recall are packed in 100-count bottles. See product images. To best identify the product, the NDC’s, Product Description, Lot Numbers and Expiration Dates are listed. These lots were distributed nationwide in the USA to Acella’s direct accounts, including wholesalers, pharmacies, and healthcare offices. Additionally, consumers may be able to determine that their product is not impacted by the recall if the “use by,” “discard after,” or “expiration date” on their prescription bottle is on or after December 2020.
Product NDC Lot # Exp. Date
NP Thyroid® 15, Thyroid Tablets, USP, ¼ grain (15 mg) 42192-327-01 M327E19-1 October 2020
NP Thyroid® 120, Thyroid Tablets, USP, 2 grain (120 mg) 42192-328-01 M328F19-3 November 2020
Acella is proactively notifying its wholesalers by email and phone to discontinue distribution of the two above referenced lots being recalled and is arranging for return of all recalled products. Patients who are currently taking NP Thyroid® from the lots being recalled should not discontinue use without contacting their healthcare provider for further guidance and/or a replacement prescription.
Check the full recall details on fda.gov
Source: FDA See Less”
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bio aaa Hand Sanitizer - recalled due to Possible presence of methanol, Miami, FL, USA
Miami, FL, USA
September 3, 2020 7:00 PM
“Company name: AJR Trading LLC
Brand name: bio aaa
Product recalled: Hand Sanitizer
Reason of the recall: Possible presence of methanol
FDA Recall date: September 03, 2020
Recall details: AJR Trading is voluntarily recalling 2,004 units of lot 20DF8307 of bio aaa Advance Hand Sanitizer currentl... See Morey in US distribution, packaged in 480 mL bottles, to the consumer level. This lot of bio aaa Advance Hand Sanitizer has been tested and meets all appropriate specifications and tests. However, in an abundance of caution, these units are being recalled because of possible presence of methanol in other lots of bio aaa Advance Hand Sanitizer.
Risk Statement: Substantial methanol exposure could result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system, or death. Although all persons using these products on their hands may be at risk; young children who accidently ingest them and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning.
To date, AJR Trading has not received reports of adverse events related to this recall.
The product is used as a hand sanitizer to reduce bacteria when soap and water is not available and is packaged in 480 mL plastic bottles UPC 7502272121085. AJR Trading is recalling lot 20DF8307, expiration date April 2022. The product can be identified by the images below. Product was distributed in Miami beginning in April 2020. AJR Trading is notifying its customers by phone calls, e-mails, and letters. AJR Trading is arranging for refund and destruction of recalled products.
Consumers/distributors/retailers that have the above listed lots of bio aaa Hand Sanitizer, which is being recalled, should stop using or distributing the products immediately and mail the products to AJR Trading at the following address for refund: 814 Ponce de Leon Blvd, suite 218. Coral Gables, FL. 33134. Consumers with questions regarding this recall can contact AJR Trading by phone insert 305-302-8416 or e-mail to ajrtrading15@gmaill.com Monday to Friday from 10:00 am to 5:00 pm Central Time.
Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax. Complete and submit the report Online
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Check the full recall details on fda.gov
Source: FDA See Less”
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September 7, 2020 8:36 PM
“The CFIA announced the recall of Frank brand Milk Chocolate Covered Raisins by Canadian Tire Corporation of Canada from the marketplace due to undeclared peanut.
- Frank Milk Chocolate Covered Raisins (300 g). UPC: 6 26394 33920 7. Best Before 2021 MA 07, Lot: 07EUA | Best Before 2021 MA 13, Lot... See More: 13EUA | Best Before 2021 JL 07, Lot: 07GUB | Best Before 2021 APR 21, Lot: 21DUB | Best Before 2021 JL 08, Lot: 08GUB
Check the full recall details on the CFIA website: inspection.gc.ca
Source: CFIA See Less”
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Zanilast+ Hand sanitizer - recalled due to Product contains 1-propanol., United States
United States
August 26, 2020 4:00 PM
“Company name: Nanomateriales, SA de CV
Brand name: Zanilast+
Product recalled: Hand sanitizer
Reason of the recall: Product contains 1-propanol.
FDA Recall date: August 26, 2020
Recall details: Apodaca, Nuevo Leon, Nanomateriales is voluntarily recalling all lots of ZANILAST+ GEL, Sanitizer gel... See More, to the consumer level. FDA laboratory analysis found ZANILAST+ GEL to contain 1-propanol.
Risk Statement: There is a reasonable probability of acute toxicity from ingestion which can cause central nervous system depression, which could result in death, permanent impairment, or necessitate medical or surgical intervention. Populations most at risk include individual with alcohol addiction and adolescents, who have been known to ingest ethanol-based antiseptic rubs intentionally to become intoxicated, as well as infants and children who may unintentionally ingest the defective product.
Nanomateriales, SA de CV has not received any reports of adverse events related to this recall. The product is used as a sanitizer gel, for hand washing to decrease bacteria on the skin and is packaged in 1 liter, 25 liters, and 1 gallon plastic bottles distributed from 05/29/2020 to 06/17/2020 in the States of California, New York and New Jersey.
Presentatio UPC NDC Lable
1 Liter 2 000000 531151 69912-008-01 See below
25 Liter 2 000000 531151 69912-006-01 See below
1 galon 2 000000 531144 69912-008-02 See below
Nanomateriales, SA de CV is notifying its distributors and customers by e-mail and phone and is arranging for return of all recalled products. Consumers and distributors that have ZANILAST+ GEL which is being recalled should return to place of purchase.
Check the full recall details on fda.gov
Source: FDA See Less”
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Nature-Throid and WP Thyroid - recalled due to Product may be sub potent, United States
United States
September 4, 2020 7:00 AM
“Company name: RLC Labs, Inc
Brand name: RLC Labs
Product recalled: Nature-Throid® and WP Thyroid®
Reason of the recall: Product may be sub potent
FDA Recall date: September 02, 2020
Recall details: RLC Labs, Inc. is voluntarily recalling a total of 483 lots of Nature-Throid® and WP Thyroid® in... See Moreall strengths, all counts of product within current expiry to the consumer level. The products are being recalled because testing of samples from six (6) lots by the U.S. Food and Drug Administration found the samples to be sub potent. The product may have as low as 87% of the labeled amount of Liothyronine (T3) or Levothyroxine(T4).
Risk Statement: Patients being treated for hypothyroidism (underactive thyroid), who receive sub potent Nature-Throid® or WP Thyroid®, may experience signs and symptoms of hypothyroidism (underactive thyroid) which may include, fatigue, increased sensitivity to cold, constipation, dry skin, puffy face, hair loss, slow heart rate, depression, swelling of the thyroid gland and/or unexplained weight gain or difficulty losing weight. There is reasonable risk of serious injury in newborn infants or pregnant women with hypothyroidism including early miscarriage, fetal hyperthyroidism, and/or impairments to fetal neural and skeletal development. In elderly patients and patients with underlying cardiac disease toxic cardiac manifestations of hyperthyroidism may occur, such as cardiac pain, palpitations or cardiac arrhythmia.
RLC Labs, Inc. has not received any reports of adverse events related to this recall. Nature-Throid® and WP Thyroid® (thyroid tablets, USP) is composed of liothyronine and levothyroxine, and are used to treat hypothyroidism (underactive thyroid). The products subject to recall are packaged in 30, 60, 90, 100 and 1,000 count bottles. To best identify the product, the NDC’s, Product Descriptions, Lot Numbers and Expiration Dates are listed in the link below.
These lots were distributed nationwide in the USA to RLC Labs, Inc.’s direct accounts, including healthcare professionals and retail pharmacies. RLC Labs, Inc. is proactively notifying its wholesalers by email, mail and phone to discontinue distribution of the product being recalled and is arranging for the return of all recalled products. Patients who are currently taking Nature-Throid® and WP Thyroid® should not discontinue use without contacting their healthcare provider for further guidance and/or replacement prescription.
Consumers with questions about the recall can email RLC Labs, Inc. at recall@rlclabs.com or contact RLC Labs, Inc. Customer Service at 1-877-797-7997, Monday through Thursday from 7:00 am to 4:00 pm MST (AZ) and Friday from 7:00 am to 3:00 pm MST (AZ). Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax. Complete and submit the report Online.
Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Check the full recall details on fda.gov
Source: FDA See Less”
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Ready-To-Eat Chicken Salad Products -recalled due to Misbranding and an Undeclared Allergen, USA
USA
September 16, 2020 9:38 PM
“The FSIS announced the recall of approximately 6,890 pounds of ready-to-eat (RTE) chicken salad products by Willow Tree Poultry Farm, Inc due to misbranding and an undeclared allergen. The products may contain walnuts, a known allergen, which are not declared on the product labels. There have been n... See Moreo confirmed reports of adverse reactions due to consumption of these products to date.
FSIS advises consumers not to eat the recalled products and to throw them away or return them to the place of purchase. The RTE chicken salad product labeled as “Classic Chicken Salad” may actually contain “White Meat Cranberry Walnut Chicken Salad” and was produced on Sept. 2, 2020. The products subject to recall bear establishment number “EST. P-8827” inside the USDA mark of inspection. These items were shipped to retail locations in Connecticut, the District of Columbia, Maine, Maryland, Massachusetts, New Hampshire, Rhode Island, Vermont and Virginia. The following products are subject to recall:
- 15-oz. clear, plastic containers labeled as “Willow Tree Premium White Meat CHICKEN SALAD Classic” with a sell by date of “9/30/20” and a time stamp of 13:00:00 through 17:00:00 on the containers’ cellophane lid.
Check the full recall details on the FSIS website fsis.usda.gov
Source: FSIS See Less”
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Trader Joe’s Southwest Style Sweet Potato Saute Bowl - recalled due to Undeclared milk and egg, USA
USA
September 21, 2020 5:00 PM
“Company name: GHSW, LLC
Brand name: Trader Joe’s
Product recalled: Southwest Style Sweet Potato Saute Bowl
Reason of the recall: Undeclared milk and egg
FDA Recall date: September 21, 2020
Recall details: GHSW, LLC. is voluntarily recalling 1512 units of Trader Joe’s Southwest Style Sweet Pot... See Moreato Sauté Bowl due to undeclared milk and egg allergens in the dressing that are not declared on the label. People who are allergic to milk and eggs run the risk of serious or life-threatening allergic reaction if they consume this product.
The dressing is located in a pouch found inside the clear 21.5 oz. bowl. These bowls are sold in the refrigerated section of the store. The recalled product(s) were shipped to 36 Trader Joe’s stores in the following states: AR, CO, KS, LA, NM, OK, TN, and TX. The recall has been isolated to only Southwest Style Sweet Potato Sauté Bowl with the Best By dates 09/23/20, 09/24/20, 09/25/20, 09/26/20, and 09/28/20 on the front of the package.
No other products or lots are affected by this recall. No reports of illnesses or injury have been received to date. The recall was initiated after it was discovered that the dressing containing milk and egg was distributed in packaging that did not declare the presence of milk or egg. GHSW, LLC is urging customers with any milk and egg allergy concerns to return the product to the point of purchase for a full refund or dispose of the recalled products. GHSW is standing by to answer customer questions at 888-449-9386, M-F, 9 am to 4 pm PST.
Check the full recall details on fda.gov
Source: FDA See Less”
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September 1, 2020 4:38 PM
“The FSIS announced the recall of approximately 1,202 pounds of ready-to-eat (RTE) chicken salad product by Ukrop’s Homestyle Foods due to misbranding and an undeclared allergen. The product may contain almonds, a known allergen, which are not declared on the product label.
The RTE chicken salad i... See Moretem was produced on August 26, 2020. The following product is subject to recall:
- 15-oz. round plastic containers containing “Ukrop’s Chicken Salad” with a sell by date of “09/02/20”.
The product subject to recall bears establishment number “P-19979” inside the USDA mark of inspection. These items were shipped to retail locations in North Carolina, Ohio, Virginia, and West Virginia. The problem was discovered after the firm received a consumer complaint reporting that the product contained almonds.
There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.
FSIS is concerned that some product may be in retailer and consumers’ refrigerators. Retailers who have obtained these products are urged not to sell them. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.
FSIS routinely conducts recall effectiveness checks to verify that recalling firms are notifying their customers of the recall and that actions are being taken to make certain that the product is no longer available to consumers. Consumers and members of the media with questions about the recall can contact Susan Rowe, Executive Administrator, Ukrop’s Homestyle Foods, at (804) 340-3050.
Check the full recall details on the FSIS website fsis.usda.gov
Source: FSIS See Less”
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September 1, 2020 4:36 PM
“Fresco Foods Inc. of Tampa, FL is voluntarily recalling ALL units of Ancient Grain Jackfruit Bowl sold at Publix because it may contain an undeclared allergen, FISH (anchovies). People who have an allergy or severe sensitivity to FISH (anchovies) run the risk of serious or life-threatening allergic... See Morereaction if they consume these products.
The allergy alert was initiated after it was discovered that the Ancient Grain Jackfruit Bowl containing Fish was distributed in packaging that did not reveal the presence of fish. Subsequent investigation indicates the problem was caused by sourcing the wrong sub-ingredient.
- Eat Fresco Ancient Grain Jackfruit Bowl. GTIN: 85898800510. Lot/Exp. Date: ALL
Individuals with an allergy or sensitivity to fish (anchovies) should not consume this product. Households that include individuals with an allergy or sensitivity to fish (anchovies) should dispose of the product or return it to the place of purchase for a refund.
Consumers with questions may contact Fresco Foods, Inc. at (813) 551-2100.
Check the full recall details on corporate.publix.com
Source: Publix See Less”
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